1W30
PyrR of Mycobacterium Tuberculosis as a potential drug target
1W30 の概要
| エントリーDOI | 10.2210/pdb1w30/pdb |
| 分子名称 | PYRR BIFUNCTIONAL PROTEIN (2 entities in total) |
| 機能のキーワード | pyrr, transferase, glycosyltransferase, psi, protein structure initiative, tb structural genomics consortium, tb, tbsgc |
| 由来する生物種 | MYCOBACTERIUM TUBERCULOSIS |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 43259.19 |
| 構造登録者 | Kantardjieff, K.A.,Vasquez, C.,Castro, P.,Warfel, N.N.,Rho, B.-S.,Lekin, T.,Kim, C.-Y.,Segelke, B.W.,Terwilliger, T.,Rupp, B.,TB Structural Genomics Consortium (TBSGC) (登録日: 2004-07-11, 公開日: 2004-09-29, 最終更新日: 2023-12-13) |
| 主引用文献 | Kantardjieff, K.A.,Vasquez, C.,Castro, P.,Warfel, N.N.,Rho, B.-S.,Lekin, T.,Kim, C.-Y.,Segelke, B.W.,Terwilliger, T.,Rupp, B. Structure of Pyrr (Rv1379) from Mycobacterium Tuberculosis: A Persistence Gene and Protein Drug Target Acta Crystallogr.,Sect.D, 61:355-, 2005 Cited by PubMed Abstract: The Mycobacterium tuberculosis pyrR gene (Rv1379) encodes a protein that regulates the expression of pyrimidine-nucleotide biosynthesis (pyr) genes in a UMP-dependent manner. Because pyrimidine biosynthesis is an essential step in the progression of TB, the gene product pyrR is an attractive antitubercular drug target. The 1.9 A native structure of Mtb pyrR determined by the TB Structural Genomics Consortium facilities in trigonal space group P3(1)21 is reported, with unit-cell parameters a = 66.64, c = 154.72 A at 120 K and two molecules in the asymmetric unit. The three-dimensional structure and residual uracil phosphoribosyltransferase activity point to a common PRTase ancestor for pyrR. However, while PRPP- and UMP-binding sites have been retained in Mtb pyrR, a distinct dimer interaction among subunits creates a deep positively charged cleft capable of binding pyr mRNA. In silico screening of pyrimidine-nucleoside analogs has revealed a number of potential lead compounds that, if bound to Mtb pyrR, could facilitate transcriptional attenuation, particularly cyclopentenyl nucleosides. PubMed: 15805589DOI: 10.1107/S090744490403389X 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.9 Å) |
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